Literature DB >> 9364218

The inactivation of the XP-C gene does not affect somatic hypermutation or class switch recombination of immunoglobulin genes.

H M Shen1, D L Cheo, E Friedberg, U Storb.   

Abstract

The mechanism of somatic hypermutation of immunoglobulin genes is not known, but appears to be linked to transcription and perhaps DNA repair. In order to determine if global DNA repair or the repair of the nontranscribed DNA strand is required for somatic mutation, we have analysed mice whose XP-C gene was inactivated by homologous recombination. Our study shows that hypermutation occurs in XP-C knockout mice with a normal frequency, suggesting that the XP-C gene product is not required for somatic hypermutation. Furthermore, we found that Ig gene switch recombination also is normal in these mice.

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Year:  1997        PMID: 9364218     DOI: 10.1016/s0161-5890(97)00064-3

Source DB:  PubMed          Journal:  Mol Immunol        ISSN: 0161-5890            Impact factor:   4.407


  9 in total

Review 1.  Altered spectra of hypermutation in DNA repair-deficient mice.

Authors:  D B Winter; P J Gearhart
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2001-01-29       Impact factor: 6.237

Review 2.  Transcription, beta-like DNA polymerases and hypermutation.

Authors:  C A Reynaud; S Frey; S Aoufouchi; A Faili; B Bertocci; A Dahan; E Flatter; F Delbos; S Storck; C Zober; J C Weill
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2001-01-29       Impact factor: 6.237

3.  Nucleotide excision repair in an immunoglobulin variable gene is less efficient than in a housekeeping gene.

Authors:  Rudaina H Alrefai; David B Winter; Vilhelm A Bohr; Patricia J Gearhart
Journal:  Mol Immunol       Date:  2007-03-01       Impact factor: 4.407

4.  B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes.

Authors:  N Kim; K Kage; F Matsuda; M P Lefranc; U Storb
Journal:  J Exp Med       Date:  1997-08-04       Impact factor: 14.307

5.  Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2.

Authors:  D B Winter; Q H Phung; A Umar; S M Baker; R E Tarone; K Tanaka; R M Liskay; T A Kunkel; V A Bohr; P J Gearhart
Journal:  Proc Natl Acad Sci U S A       Date:  1998-06-09       Impact factor: 11.205

6.  Different mismatch repair deficiencies all have the same effects on somatic hypermutation: intact primary mechanism accompanied by secondary modifications.

Authors:  N Kim; G Bozek; J C Lo; U Storb
Journal:  J Exp Med       Date:  1999-07-05       Impact factor: 14.307

7.  The role of DNA repair in somatic hypermutation of immunoglobulin genes.

Authors:  N Kim; U Storb
Journal:  J Exp Med       Date:  1998-06-01       Impact factor: 14.307

8.  Reduced isotype switching in splenic B cells from mice deficient in mismatch repair enzymes.

Authors:  C E Schrader; W Edelmann; R Kucherlapati; J Stavnezer
Journal:  J Exp Med       Date:  1999-08-02       Impact factor: 14.307

9.  A hypermutable insert in an immunoglobulin transgene contains hotspots of somatic mutation and sequences predicting highly stable structures in the RNA transcript.

Authors:  U Storb; E L Klotz; J Hackett; K Kage; G Bozek; T E Martin
Journal:  J Exp Med       Date:  1998-08-17       Impact factor: 14.307

  9 in total

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